Status:
COMPLETED
Integrating Electronic Patient Reported Biometric Measures (ePReBMs) From Wearable Devices in Respiratory Diseases
Lead Sponsor:
University of Alberta
Conditions:
Progressive Fibrosing Interstitial Lung Disease
Lung Transplant
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Lung diseases are one of the most common causes of emergency room visits. There are very few tools that are able to predict which patients will have a worsening or increasing severity of their conditi...
Detailed Description
The project will aim to create the infrastructure to collect clinical data and participants reported biometric measures (ePReBMs) from wearable devices in a database, and to run a pilot phase with a l...
Eligibility Criteria
Inclusion
- Patients with PF-ILD (including IPF), lung transplant, CF, bronchiectasis or TB must meet all of the following criteria to be enrolled in the study:
- Male or female volunteers, at least 18 years of age at the time of screening visit;
- Fluent in English and able to follow the instructions to use the ADAMM-RSM™;
- Willing and cognitively able to sign informed consent
Exclusion
- Patients must be excluded from participation in this study if any of the following criteria are met:
- Pregnancy;
- History of active (clinically significant) skin disorders;
- History of allergic response to silicones or adhesives;
- Subjects with electronic implants of any kind (e.g. pacemaker);
- Broken, damaged or irritated skin or rashes near the sensor application sites;
- Subjects who are physically or cognitively unable to normally perform activities of daily living, assessed at the discretion of the investigator.
Key Trial Info
Start Date :
July 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2023
Estimated Enrollment :
8 Patients enrolled
Trial Details
Trial ID
NCT04857814
Start Date
July 1 2021
End Date
March 1 2023
Last Update
April 19 2023
Active Locations (1)
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1
University of Alberta
Edmonton, Alberta, Canada, T6G 2B7